Provicol QM Plus
K 號：K161630 · 2016-09-15
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器材摘要
Provicol QM Plus is the device name listed in this FDA 510(k) record. The listed applicant is Voco GmbH. It received FDA 510(k) clearance on 2016-09-15 under 510(k) number K161630. The device is classified under product code EMB. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.
常見問題
What is the Provicol QM Plus?
Provicol QM Plus is a medical device that received FDA 510(k) clearance on 2016-09-15. The listed applicant is Voco GmbH. The 510(k) number is K161630.
When did Provicol QM Plus receive FDA 510(k) clearance?
Provicol QM Plus received FDA 510(k) clearance on 2016-09-15, under 510(k) number K161630.
Who is the listed applicant for Provicol QM Plus?
The FDA 510(k) record lists Voco GmbH as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for Provicol QM Plus?
The FDA product code for Provicol QM Plus is EMB.
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其他以 Voco GmbH 為申請人之記錄
相關紀錄係使用名稱、產品代碼或其他後設資料自動配對。配對結果並不構成已驗證的臨床、科學、企業或監管關係，請查閱連結的官方來源。
官方來源
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